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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 2851 - 2875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0060074 ductal carcinoma in situ HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:9306962
DOID:1793 pancreatic cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19671868
DOID:3744 cervical squamous cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:16803522
DOID:1380 endometrial cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:18348659
DOID:2671 transitional cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:15841086
DOID:4608 common bile duct neoplasm HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:10760693
DOID:11054 urinary bladder cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:16937303
DOID:3908 lung non-small cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19671868
DOID:2394 ovarian cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:15262124
  • PMID:15628771
DOID:4450 renal cell carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:12614261
  • PMID:16861722
DOID:890 mitochondrial encephalomyopathy HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:9924029
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:9884 muscular dystrophy WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110444 dilated cardiomyopathy 1X WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 WB:WBGene00020924 Caenorhabditis elegans 189104 W02B3.4
  • MGI:6194238
DOID:14500 fucosidosis WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:8947 diabetic retinopathy WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238
DOID:9351 diabetes mellitus WB:WBGene00012225 Caenorhabditis elegans 189173 W03G11.3
  • MGI:6194238

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